首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis, antibacterial and antiviral properties of curcumin bioconjugates bearing dipeptide, fatty acids and folic acid.
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Synthesis, antibacterial and antiviral properties of curcumin bioconjugates bearing dipeptide, fatty acids and folic acid.

机译:具有二肽,脂肪酸和叶酸的姜黄素生物共轭物的合成,抗菌和抗病毒特性。

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摘要

Curcumin bioconjugates, viz. di-O-tryptophanylphenylalanine curcumin (2), di-O-decanoyl curcumin (3), di-O-pamitoyl curcumin (4), di-O-bis-(gamma,gamma)folyl curcumin (6), C(4)-ethyl-O-gamma-folyl curcumin (8) and 4-O-ethyl-O-gamma-folyl curcumin (10) have been synthesized and tested for their antibacterial and antiviral activities. The conjugates 2, 3, 4, 6 and 8 have shown very promising antibacterial activity with MIC ranging between 0.09 and 0.67 microM against Gram-positive cocci and Gram-negative bacilli. Further, the conjugates 2, 3, 6, 8 and 10 have been screened for their antiviral activities against HSV, VSV, FIPV, PIV-3, RSV and FHV and the molecules 2 and 3 have shown good results with EC(50) 0.011 microM and 0.029 microM against VSV and FIPV/FHV, respectively. However, the molecules did not show expected results against HIV-1 III(B) and ROD strains in MTT assay.
机译:姜黄素生物缀合物,即。二-O-色氨酸基苯丙氨酸姜黄素(2),二-O-癸酰姜黄素(3),二-O-戊酰姜黄素(4),二-O-双-(γ,γ)叶酰姜黄素(6),C(4 )-乙基-O-γ-叶姜黄素(8)和4-O-乙基-O-γ-叶姜黄素(10)已合成并测试了其抗菌和抗病毒活性。结合物2、3、4、6和8显示出非常有前途的抗菌活性,其MIC对革兰氏阳性球菌和革兰氏阴性杆菌的范围为0.09至0.67μM。此外,已针对缀合物2、3、6、8和10筛选了针对HSV,VSV,FIPV,PIV-3,RSV和FHV的抗病毒活性,并且分子2和3在EC(50)0.011下显示出良好的结果分别针对VSV和FIPV / FHV的microM和0.029 microM。但是,该分子在MTT分析中未显示出针对HIV-1 III(B)和ROD菌株的预期结果。

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